Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2009-3-24
pubmed:abstractText
To use a combined neurogenetic-neuroimaging approach to examine the functional consequences of preclinical dopaminergic nigrostriatal dysfunction in the human motor system. Specifically, we examined how a single heterozygous mutation in different genes associated with recessively inherited Parkinson disease alters the cortical control of sequential finger movements.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-10094257, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-10234047, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-11261512, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-11921141, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-11976394, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-12244082, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-12446870, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-12447943, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-12832556, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-14573560, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-14673808, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-15349860, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-15642918, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-15947065, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-16130111, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-16672980, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-16672981, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-16753182, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-16769864, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-16914982, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-17013904, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-17237780, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-17582365, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-17724286, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-17913900, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-18003639, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-19307537, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-5146491, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-7507940, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-7515081, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-9217681, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-9391021, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-9463462, http://linkedlifedata.com/resource/pubmed/commentcorrection/19038850-9560156
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
24
pubmed:volume
72
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1041-7
pubmed:dateRevised
2010-9-22
pubmed:meshHeading
pubmed-meshheading:19038850-Adaptation, Biological, pubmed-meshheading:19038850-Adult, pubmed-meshheading:19038850-Biological Markers, pubmed-meshheading:19038850-Brain Mapping, pubmed-meshheading:19038850-Female, pubmed-meshheading:19038850-Frontal Lobe, pubmed-meshheading:19038850-Genetic Predisposition to Disease, pubmed-meshheading:19038850-Heterozygote, pubmed-meshheading:19038850-Heterozygote Detection, pubmed-meshheading:19038850-Humans, pubmed-meshheading:19038850-Magnetic Resonance Imaging, pubmed-meshheading:19038850-Male, pubmed-meshheading:19038850-Middle Aged, pubmed-meshheading:19038850-Motor Cortex, pubmed-meshheading:19038850-Movement, pubmed-meshheading:19038850-Mutation, pubmed-meshheading:19038850-Neuronal Plasticity, pubmed-meshheading:19038850-Parkinsonian Disorders, pubmed-meshheading:19038850-Phenotype, pubmed-meshheading:19038850-Protein Kinases, pubmed-meshheading:19038850-Ubiquitin-Protein Ligases
pubmed:year
2009
pubmed:articleTitle
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.
pubmed:affiliation
Department of Neurology, Christian-Albrechts University, Kiel, Germany.
pubmed:publicationType
Journal Article
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